TY - JOUR
T1 - Polycomb group gene mel-18 regulates early T progenitor expansion by maintaining the expression of Hes-1, a target of the notch pathway
AU - Miyazaki, Masaki
AU - Kawamoto, Hiroshi
AU - Kato, Yuko
AU - Itoi, Manami
AU - Miyazaki, Kazuko
AU - Masuda, Kyoko
AU - Tashiro, Satoshi
AU - Ishihara, Hiroto
AU - Igarashi, Kazuhiko
AU - Amagai, Takashi
AU - Kanno, Rieko
AU - Kanno, Masamoto
PY - 2005/3/1
Y1 - 2005/3/1
N2 - Polycomb group (PcG) proteins play a role in the maintenance of cellular identity throughout many rounds of cell division through the regulation of gene expression. In this report we demonstrate that the loss of the PcG gene mel-18 impairs the expansion of the most immature T progenitor cells at a stage before the rearrangement of the TCR β-chain gene in vivo and in vitro. This impairment of these T progenitors appears to be associated with increased susceptibility to cell death. We also show that the expression of Hes-1, one of the target genes of the Notch signaling pathway, is drastically down-regulated in early T progenitors isolated from mel-18-/- mice. In addition, mel-18-/- T precursors could not maintain the Hes-1 expression induced by Delta-like-1 in monolayer culture. Collectively, these data indicate that mel-18 contributes to the maintenance of the active state of the Hes-1 gene as a cellular memory system, thereby supporting the expansion of early T progenitors.
AB - Polycomb group (PcG) proteins play a role in the maintenance of cellular identity throughout many rounds of cell division through the regulation of gene expression. In this report we demonstrate that the loss of the PcG gene mel-18 impairs the expansion of the most immature T progenitor cells at a stage before the rearrangement of the TCR β-chain gene in vivo and in vitro. This impairment of these T progenitors appears to be associated with increased susceptibility to cell death. We also show that the expression of Hes-1, one of the target genes of the Notch signaling pathway, is drastically down-regulated in early T progenitors isolated from mel-18-/- mice. In addition, mel-18-/- T precursors could not maintain the Hes-1 expression induced by Delta-like-1 in monolayer culture. Collectively, these data indicate that mel-18 contributes to the maintenance of the active state of the Hes-1 gene as a cellular memory system, thereby supporting the expansion of early T progenitors.
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U2 - 10.4049/jimmunol.174.5.2507
DO - 10.4049/jimmunol.174.5.2507
M3 - Article
C2 - 15728456
AN - SCOPUS:20044371985
SN - 0022-1767
VL - 174
SP - 2507
EP - 2516
JO - Journal of Immunology
JF - Journal of Immunology
IS - 5
ER -